Primary Device ID | 30808232001243 |
NIH Device Record Key | d6aa766b-49d9-4310-8f8b-1cd79d10d1c2 |
Commercial Distribution Discontinuation | 2018-06-30 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | VitaPrep |
Version Model Number | 2113-0013 |
Catalog Number | 2113-0013 |
Company DUNS | 149183167 |
Company Name | Stryker Corporation |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | true |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(610)640-1775 |
obxsharedservices@stryker.com | |
Phone | +1(610)640-1775 |
obxsharedservices@stryker.com |
Storage Environment Temperature | Between 20 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 20 Degrees Celsius and 30 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00808232001242 [Primary] |
GS1 | 30808232001243 [Package] Contains: 00808232001242 Package: pack [5 Units] Discontinued: 2018-06-30 Not in Commercial Distribution |
LMF | Agent, absorbable hemostatic, collagen based |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-04-23 |
Device Publish Date | 2014-09-24 |
07613327634914 - Neptune | 2024-04-24 SMART DOCKING STATION (120V) |
07613327627664 - KNOTILUS+ | 2024-03-15 2.9X12.5MM KNOTILUS+ HIP ANCHOR - PEEK |
07613327627701 - KNOTILUS+ | 2024-03-15 2.4X8.9MM KNOTILUS+ HIP ANCHOR - PEEK |
07613327623796 - KNOTILUS+ | 2024-03-13 2.4X8.9MM DRILL, HIP |
07613327623833 - KNOTILUS+ | 2024-03-13 2.4X8.9MM DRILL, HARD BONE, HIP |
07613327634686 - Iconix | 2024-03-12 Iconix DC Guide for 1.4mm anchor |
07613327634693 - Iconix | 2024-03-12 |
07613327616675 - SPY | 2024-03-06 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VITAPREP 86700430 4895833 Live/Registered |
PregPrep LLC 2015-07-21 |
VITAPREP 85182050 4289501 Live/Registered |
Orthovita, Inc. 2010-11-22 |